Academic literature on the topic 'Potato virus M - composition'

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Journal articles on the topic "Potato virus M - composition"

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He, Zhen, Haifeng Gan, and Xinyan Liang. "Analysis of Synonymous Codon Usage Bias in Potato Virus M and Its Adaption to Hosts." Viruses 11, no. 8 (2019): 752. http://dx.doi.org/10.3390/v11080752.

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Potato virus M (PVM) is a member of the genus Carlavirus of the family Betaflexviridae and causes large economic losses of nightshade crops. Several previous studies have elucidated the population structure, evolutionary timescale and adaptive evolution of PVM. However, the synonymous codon usage pattern of PVM remains unclear. In this study, we performed comprehensive analyses of the codon usage and composition of PVM based on 152 nucleotide sequences of the coat protein (CP) gene and 125 sequences of the cysteine-rich nucleic acid binding protein (NABP) gene. We observed that the PVM CP and
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Kim, Irina, Elena Barsukova, Petr Fisenko, et al. "Applying methods of replication and recovery of potato microplants (Solanum tuberosum l.) in seed production." E3S Web of Conferences 203 (2020): 02003. http://dx.doi.org/10.1051/e3sconf/202020302003.

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Potatoes are strongly affected by pests and by pathogens of fungal, bacterial and viral nature. The most common and economically significant potato viruses are Y (PVY), X (PVX), S (PVS), M (PVM), and potato leaf twisting virus (PLRV). The development of a virus-free bio-resource collection in vitro is the basis for plant breeding development and transferring seed production to a healthier foundation. In this regard, the aim of this research was to apply methods of recovery and select optimal conditions for in vitro propagation of a collection of virus-free potato varieties. A collection of 22
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Reshotko, L. M., O. O. Dmitruk, and I. V. Volkova. "SPREAD OF VIRAL DISEASES OF POTATOES IN AGROCENOSIS OF THE CARPATHIAN ECONOMIC AREA." Agriciltural microbiology 30 (December 3, 2019): 54–60. http://dx.doi.org/10.35868/1997-3004.30.54-60.

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Objective. Determine the phytovirological condition of potato crops in the agrocenosis of Carpathian economic area on the basis of obtaining and systematisation of data on the composition of the viral population. Methods. The methods of visual and serological diagnostics, electronic microscopy (EM) of native specimens, biotesting were used to detect and identify potato viruses. For carrying out serological analyses, antisera were used to detect potato viruses obtained in the Virology Laboratory of the Institute of Agricultural Microbiology and Agroindustrial Manufacture of the National Academy
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Lambert, Susan J., Frank S. Hay, Sarah J. Pethybridge, and Calum R. Wilson. "Spatiotemporal Spread of Potato virus S and Potato virus X in Seed Potato in Tasmania, Australia." Plant Health Progress 8, no. 1 (2007): 70. http://dx.doi.org/10.1094/php-2007-0726-07-rs.

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The spatial and temporal distribution of Potato virus S (PVS) and Potato virus X (PVX) was studied in two trials within each of four commercial fields of seed potato var. Russet Burbank in Tasmania, Australia. In the first trial (plots) 20 leaflets were collected from each of 49 plots (each approximately 8 m wide by 10 m long), with plots arranged in a 7-×-7 lattice. In the second trial (transects), leaflets were collected at 1-m intervals along seven adjacent, 50-m long rows. The mean incidence of PVS increased during the season by 5.2% in one of four plot trials and 25.5% in one of four tran
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Proll, Eckhard, and Heinz B. Schmidt. "Stabilisierung des Kartoffel-M-Virus (potato virus M)in vitrodurch zweiwertige Ionen." Archives Of Phytopathology And Plant Protection 26, no. 2 (1990): 115–24. http://dx.doi.org/10.1080/03235409009438955.

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Tatarowska, Beata, Jarosław Plich, Dorota Milczarek, and Bogdan Flis. "Temperature‐dependent resistance to potato virus M in potato ( Solanum tuberosum )." Plant Pathology 69, no. 8 (2020): 1445–52. http://dx.doi.org/10.1111/ppa.13245.

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Zavriev, S. K., K. V. Kanyuka, and K. E. Levay. "The Genome Organization of Potato Virus M RNA." Journal of General Virology 72, no. 1 (1991): 9–14. http://dx.doi.org/10.1099/0022-1317-72-1-9.

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Kalnciema, Ieva, Ina Balke, Dace Skrastina, Velta Ose, and Andris Zeltins. "Potato Virus M-Like Nanoparticles: Construction and Characterization." Molecular Biotechnology 57, no. 11-12 (2015): 982–92. http://dx.doi.org/10.1007/s12033-015-9891-0.

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Ahmadvand, R., A. Takács, J. Taller, I. Wolf, and Z. Polgár. "Potato viruses and resistance genes in potato." Acta Agronomica Hungarica 60, no. 3 (2012): 283–98. http://dx.doi.org/10.1556/aagr.60.2012.3.10.

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Potato (Solanum tuberosum L.) is the fourth most important food crop in the world. It is the most economically valuable and well-known member of the plant family Solanaceae. Potato is the host of many pathogens, including fungi, bacteria, Phytoplasmas, viruses, viroids and nematodes, which cause reductions in the quantity and quality of yield. Apart from the late blight fungus [Phytophthora infestans (Mont.) de Bary] viruses are the most important pathogens, with over 40 viruses and virus-like pathogens infecting cultivated potatoes in the field, among which Potato virus Y (PVY), Potato leaf r
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Chaudhary, Poonam, Reenu Kumari, Balwinder Singh, Vipin Hallan, and Avinash Kaur Nagpal. "First report of potato virus M, potato virus Y and cucumber mosaic virus infection in Solanum nigrum in India." Journal of Plant Pathology 101, no. 2 (2018): 419. http://dx.doi.org/10.1007/s42161-018-0194-8.

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Dissertations / Theses on the topic "Potato virus M - composition"

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Vaculík, Petr. "Molekulárně-biologická charakterizace M viru bramboru a viru svinutky bramboru." Master's thesis, 2011. http://www.nusl.cz/ntk/nusl-297173.

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The main aims of diploma thesis were: 1) The sequence analysis of the Czech isolate of Potato virus M (PVM) VIRUBRA 4/009 and phylogenetic analysis of PVM coat proteins sequences 2) The bacterial expression of recombinant triple gene block protein 1 (TGB1) of PVM derived from the Czech isolate VIRUBRA 4/007 3) The construction of expression cassette of Potato leafroll virus (PLRV) coat protein and its transformation into A. tumefaciens for transgenic PLRV resistant plant formation In theoretical part of the thesis the taxonomic classification, morphology, genomic structure and virus transmissi
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Book chapters on the topic "Potato virus M - composition"

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Brunt, Alan A. "Potato Virus M (PVM; Genus Carlavirus)." In Virus and Virus-like Diseases of Potatoes and Production of Seed-Potatoes. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-007-0842-6_10.

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"maize, 1.4-2.7%; of waxy barley, 2.1-8.3%; and of waxy swell only slightly in cold water. Granules differ in size rice 0-2.3%; thus the range of amylose contents of the and shape among plants. For example, corn starch has an waxy wheats is comparable to that of other waxy cereal average diameter of about 15 1.1,M, wheat starch has a bi-grains. Biochemical features of starch from waxy wheats modal size distribution of 25-40 and 5-10 [tm, potato are similar to those of waxy maize [71]. starch has an average size of 40 WTI, and rice starch has an Starch from barley contains 22-26% amylose, the rest average size of 5µm [99]. being amylopectin [28]. However, samples of 11-26% The particle sizes of starch granules have recently re-amylose are known, and starch from waxy barley contains ceived much attention because of their important roles in only 0-3% amylose, while high-amylose starches contain determining both the taste and mouthfeel of fat substitutes up to 45%. and the tensible properties of degradable plastic films. Amylose content of rice is categorized as very low Daniel and Whistler [39] reported that small-granule (0-9%), low (9-20%), intermediate (20-25%), or high starch about 2 !um in diameter, or similar in size to the lipid (25-33%) [124]. The amylose content of long grain rice micelle, had advantages as a fat substitute. Lim et al. [117] ranges from 23 to 26%, while medium grain ranges from investigated the use of starches of different particle size in 15 to 20% and short grain ranges from 18 to 20% [103]. degradable plastic film. They reported that a linear correla-Oat amylose content (16-27%) is similar to that of tion between film thickness and particle size and an in-wheat starch, but oat amylose is more linear and oat amy-verse linear correlation between film thickness and particle lopectin is more branched than that found in wheat [121]. size. Small-granule starches may also be used as face pow-Most sorghum starch is similar in composition to corn der or dusting powder, as a stabilizer in baking powder, and contains 70-80% branched amylopectin and 21-28% and as laundry-stiffening agents. amylose [127]. However, waxy or glutinous sorghum con-The size of the wheat starch granule is 1-30 lam, the tains starch with 100% amylopectin and has unique prop-size distribution being bimodal. Such a bimodal size distri-erties similar to waxy corn [158]. Badi et al. [11] reported bution is characteristic of wheat starch, as well as of rye 17% amylose in starch from one pearl milled population. and barley starches. Wheat starch consists of two basic Gracza [69] reviewed the minor constituents of starch. forms: small spherical granules (about 5-10 wri) and larg-Cereal starches contain low levels of lipids. Usually, the er lenticular granules (about 25-4011m). The small B-gran-lipids associated with starch are polar lipids. Generally, the ules are spherical and have a diameter of less than 10 wrt; level of lipids in cereal starch is between 0.5 and 1%. Be-a mean value of about 4 lam has been reported. The large sides low levels of other minerals, starches contain phos-A-granules are lenticular and have a diameter greater than phorus and nitrogen. In the cereals, phosphorus occurs 10 lam, with a mean 14.11.1m. In reality, the granules have a mostly in the form of phospholipids. The nitrogen is gener-continuous distribution of granule size within the range ally considered to be present as protein, but it may also be designated for that starch. Amylose and amylopectin are a constituent of the lipid fraction. intermixed and distributed evenly throughout the granule. The interaction between amylose and lipids is more Many believe that the composition and properties of small powerful by far than that between amylopectin and lipids and large granules are similar, but this is a subject of some [55]. It is well established that polar lipids (e.g., mono-argument and the subject of many research studies [42]. glycerides, fatty acids, and similar compounds) form a hel-Kulp [110] evaluated the fundamental and bread-mak-ical inclusion complex with the amylose molecule, be-ing properties of small wheat starch granules and com-tween the hydrocarbon chain of the lipid and the interior of pared them with those of regular starch. Small granules the amylose helix. were found to be lower in iodine affinity, indicating differ-ences in amylose levels or some fundamental structural differences. Gelatinization temperature ranges, water-binding capacities, and enzymic susceptibilities of small Starch is laid down in the shape of particles in special amy-granules were higher than those of regular ones. loplast cells in the plant. These particles are called gran-Rice has one of the smallest starch granules of cereal ules, and they are the means by which the plant stores en-grains, ranging in size from 3 to 5 pm in the mature grain, ergy for the carbohydrate in a space-saving way, but also to although the small granules of wheat starch are almost the make the energy easily accessible when the seed germi-same size [33]. The small granule size of that starch results nates [57]. One starch granule is synthesized in each amy-in physical properties that make it useful as a dusting flour loplast, and the shape and size of a starch granule is typical in bakeries. Rice starch amyloses have degree of polymer-of its botanical origin. ization (DP) values of 1000-1100 and average chain Starch granules are relatively dense, insoluble, and lengths of 250-320. These structural properties of amylose." In Handbook of Cereal Science and Technology, Revised and Expanded. CRC Press, 2000. http://dx.doi.org/10.1201/9781420027228-41.

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Conference papers on the topic "Potato virus M - composition"

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Chin, N. V., N. H. Thai, and N. T. Thuy. "RESEARCH EFFECT OF POTATO VIRUS Y ON GROWTH, YIELD AND CHEMICAL COMPOSITION OF FLUE-CURED TOBACCO IN NORTH OF VIETNAM." In Состояние и перспективы мировых научных исследований по табаку, табачным изделиям и инновационной никотинсодержащей продукции. Государственное научное учреждение Всероссийский научно-исследовательский институт табака, махорки и табачных изделий Российской академии сельскохозяйственных наук, 2020. http://dx.doi.org/10.48113/496_2020_166-176.

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Kolychikhina, M. S. "Positive effect of preparations with antiviral properties on potato productivity." In Растениеводство и луговодство. Тимирязевская сельскохозяйственная академия, 2020. http://dx.doi.org/10.26897/978-5-9675-1762-4-2020-111.

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In the small-plot experiment of the Russian State Agrarian University - Moscow Timiryazev Agricultural Academy against potato viruses in 2014-2019 were tested some kinds of preparations with antiviral activity: Pharmayod, GS (100 g/l of iodine); Immunocytophyte, TAB (20 g/kg arachidonic acid ethyl ester); Ecogel, WS (30 g/l of chitosan lactate); Amulet, TAB (composition of linear polyaminosaccharides (chitosan) in succinic acid solution); Zerox, WS (3000 mg /l colloidal silver); Viron, WS (biostimulant based on urea and citric acid with the addition of essential oils). According to the results
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